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JPH066789B2 - Deposition method of borophosphosilicate glass - Google Patents

Deposition method of borophosphosilicate glass

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Publication number
JPH066789B2
JPH066789B2 JP60171296A JP17129685A JPH066789B2 JP H066789 B2 JPH066789 B2 JP H066789B2 JP 60171296 A JP60171296 A JP 60171296A JP 17129685 A JP17129685 A JP 17129685A JP H066789 B2 JPH066789 B2 JP H066789B2
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JP
Japan
Prior art keywords
vapor deposition
borophosphosilicate glass
oxygen
deposition method
temperature
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
JP60171296A
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Japanese (ja)
Other versions
JPS6144180A (en
Inventor
カーン ワーナー
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RCA Corp
Original Assignee
RCA Corp
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Publication date
Application filed by RCA Corp filed Critical RCA Corp
Publication of JPS6144180A publication Critical patent/JPS6144180A/en
Publication of JPH066789B2 publication Critical patent/JPH066789B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Classifications

    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
    • H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
    • H01L21/02104—Forming layers
    • H01L21/02107—Forming insulating materials on a substrate
    • H01L21/02109—Forming insulating materials on a substrate characterised by the type of layer, e.g. type of material, porous/non-porous, pre-cursors, mixtures or laminates
    • H01L21/02112—Forming insulating materials on a substrate characterised by the type of layer, e.g. type of material, porous/non-porous, pre-cursors, mixtures or laminates characterised by the material of the layer
    • H01L21/02123—Forming insulating materials on a substrate characterised by the type of layer, e.g. type of material, porous/non-porous, pre-cursors, mixtures or laminates characterised by the material of the layer the material containing silicon
    • H01L21/02126—Forming insulating materials on a substrate characterised by the type of layer, e.g. type of material, porous/non-porous, pre-cursors, mixtures or laminates characterised by the material of the layer the material containing silicon the material containing Si, O, and at least one of H, N, C, F, or other non-metal elements, e.g. SiOC, SiOC:H or SiONC
    • H01L21/02129—Forming insulating materials on a substrate characterised by the type of layer, e.g. type of material, porous/non-porous, pre-cursors, mixtures or laminates characterised by the material of the layer the material containing silicon the material containing Si, O, and at least one of H, N, C, F, or other non-metal elements, e.g. SiOC, SiOC:H or SiONC the material being boron or phosphorus doped silicon oxides, e.g. BPSG, BSG or PSG
    • C—CHEMISTRY; METALLURGY
    • C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C16/00—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
    • C23C16/22—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the deposition of inorganic material, other than metallic material
    • C23C16/30—Deposition of compounds, mixtures or solid solutions, e.g. borides, carbides, nitrides
    • C23C16/40—Oxides
    • C23C16/401—Oxides containing silicon
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
    • H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
    • H01L21/02104—Forming layers
    • H01L21/02107—Forming insulating materials on a substrate
    • H01L21/02225—Forming insulating materials on a substrate characterised by the process for the formation of the insulating layer
    • H01L21/0226—Forming insulating materials on a substrate characterised by the process for the formation of the insulating layer formation by a deposition process
    • H01L21/02263—Forming insulating materials on a substrate characterised by the process for the formation of the insulating layer formation by a deposition process deposition from the gas or vapour phase
    • H01L21/02271—Forming insulating materials on a substrate characterised by the process for the formation of the insulating layer formation by a deposition process deposition from the gas or vapour phase deposition by decomposition or reaction of gaseous or vapour phase compounds, i.e. chemical vapour deposition
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
    • H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
    • H01L21/04—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer
    • H01L21/18—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic Table or AIIIBV compounds with or without impurities, e.g. doping materials
    • H01L21/30—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26
    • H01L21/31—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26 to form insulating layers thereon, e.g. for masking or by using photolithographic techniques; After treatment of these layers; Selection of materials for these layers
    • H01L21/314—Inorganic layers
    • H01L21/316—Inorganic layers composed of oxides or glassy oxides or oxide based glass
    • H01L21/31604—Deposition from a gas or vapour
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
    • H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
    • H01L21/02104—Forming layers
    • H01L21/02107—Forming insulating materials on a substrate
    • H01L21/02109—Forming insulating materials on a substrate characterised by the type of layer, e.g. type of material, porous/non-porous, pre-cursors, mixtures or laminates
    • H01L21/02205—Forming insulating materials on a substrate characterised by the type of layer, e.g. type of material, porous/non-porous, pre-cursors, mixtures or laminates the layer being characterised by the precursor material for deposition
    • H01L21/02208—Forming insulating materials on a substrate characterised by the type of layer, e.g. type of material, porous/non-porous, pre-cursors, mixtures or laminates the layer being characterised by the precursor material for deposition the precursor containing a compound comprising Si
    • H01L21/02211—Forming insulating materials on a substrate characterised by the type of layer, e.g. type of material, porous/non-porous, pre-cursors, mixtures or laminates the layer being characterised by the precursor material for deposition the precursor containing a compound comprising Si the compound being a silane, e.g. disilane, methylsilane or chlorosilane

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Physics & Mathematics (AREA)
  • Condensed Matter Physics & Semiconductors (AREA)
  • General Physics & Mathematics (AREA)
  • Manufacturing & Machinery (AREA)
  • Computer Hardware Design (AREA)
  • Microelectronics & Electronic Packaging (AREA)
  • Power Engineering (AREA)
  • Inorganic Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Chemical Vapour Deposition (AREA)
  • Glass Melting And Manufacturing (AREA)
  • Glass Compositions (AREA)
  • Formation Of Insulating Films (AREA)
  • Internal Circuitry In Semiconductor Integrated Circuit Devices (AREA)

Description

【発明の詳細な説明】 産業上の利用分野 本発明は、電子装置に使われる硼燐珪酸ガラスの蒸着法
の改良に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to improvements in vapor deposition of borophosphosilicate glass used in electronic devices.

発明の背景 電子産業の分野において、多層の金属化構造が普通のこ
とになりつつある。この場合、最初の金属層が適当な基
板上に被着され、処理される。その上に、絶縁用誘電体
材料の層が被着され、また第１レベルの金属あるいは基
板の一部を露光するための開口が形成される。その上に
第２の金属層が被着され、相互接続系統の残りの部分を
形成するための処理が行なわれる。このような構造にお
ける誘電体材料として硼燐珪酸ガラスを使うことは、19
84年８月１６日に出願された出願番号第641,410号の出
願において、シュネイブル（Schnable）氏およびカーン
（Kern）氏により開示されている。BACKGROUND OF THE INVENTION Multilayer metallization structures are becoming commonplace in the electronics industry. In this case, the first metal layer is deposited and processed on a suitable substrate. A layer of insulating dielectric material is deposited thereover and an opening is formed for exposing a portion of the first level metal or substrate. A second metal layer is deposited thereover and processed to form the remainder of the interconnection system. The use of borophosphosilicate glass as a dielectric material in such structures is
It is disclosed by Schnable and Kern in application number 641,410 filed August 16, 1984.

硼燐珪酸ガラスの層およびこの層を半導体技術分野で使
用することについては、1969年１２月２日にカーン（Ke
rn）氏に付与された米国特許第3,481,781号明細書に開
示されている。半導体装置におけるガラス・コーティン
グにテーパー開口を形成するために硼燐珪酸ガラスを使
用することは、1982年９月１４日にフラトリー(Flatle
y)氏他に付与された米国特許第4,349,584号明細書に開
示され、また1982年１２月１４日にスー（Hsu）氏他に
付与された米国特許第4,363,830号明細書に開示されて
いる。このような応用例は、硼燐珪酸ガラスの優れた融
解−再固化特性を利用するものである。このような応用
例では、硼燐珪酸ガラスの層は、基板の上に被着され、
形状をよりよく覆うように融解して勾配がつくまで加熱
させる。開口が硼燐珪酸ガラスの層および１つもしくは
それ以上の下の層に形成される。次いで基板は、硼燐珪
酸ガラスが軟化し、開口の縁を流れるような温度まで加
熱される。このようにして良好なネーパー開口が形成さ
れる。A layer of borophosphosilicate glass and its use in the field of semiconductor technology is described on Dec. 2, 1969 in Kern (Ke).
rn) in U.S. Pat. No. 3,481,781. The use of borophosphosilicate glass to form tapered openings in glass coatings in semiconductor devices has been reported by Flatle on September 14, 1982.
y) disclosed in U.S. Pat. No. 4,349,584 to U.S. Pat. No. 4,363,830 issued Dec. 14, 1982 to Hsu et al. Such applications make use of the excellent melting-resolidifying properties of borophosphosilicate glass. In such applications, a layer of borophosphosilicate glass is deposited on the substrate,
Heat until the shape is better melted and graded. Openings are formed in the borophosphosilicate glass layer and one or more underlying layers. The substrate is then heated to a temperature such that the borophosphosilicate glass softens and flows through the edges of the opening. In this way, a good Naper opening is formed.

硼燐珪酸ガラスの層は、通常、化学蒸着法（ＣＶＤ）に
より被着される。本発明の化学蒸着法の改良によると、
硼燐珪酸ガラスの層の被着速度およびその品質が極めて
改善される。The layer of borophosphosilicate glass is usually deposited by chemical vapor deposition (CVD). According to the improved chemical vapor deposition method of the present invention,
The deposition rate of the layer of borophosphosilicate glass and its quality are greatly improved.

発明の概要 硼燐珪酸ガラスが、約３６０℃〜約３９０℃の温度で、
化学蒸着法により適当な基板上に被着される。SUMMARY OF THE INVENTION The borophosphosilicate glass has a temperature of about 360 ° C. to about 390 ° C.
It is deposited on a suitable substrate by chemical vapor deposition.

実施例 硼燐珪酸ガラスの化学蒸着法は、珪素、硼素および燐の
各水素化物、すなわちシラン（SiH4）、ホスフィン（PH
3）およびジボラン（B2H6）の混合物を適当な不活性の
希釈剤、典型的には窒素で気相酸化させることによって
実行される。酸化窒素、亜酸化窒素および二酸化炭素の
ような他の気体を使うこともできるが、酸素が最も普通
に使われる酸化体である。通常、硼燐珪酸ガラスは、約
410℃〜約450℃温度で化学蒸着法により蒸着され、約４
２５℃〜約４３０℃が最も典型的な温度である。EXAMPLE Chemical vapor deposition of borophosphosilicate glass is performed by using silicon, boron and phosphorus hydrides, that is, silane (SiH 4 ), phosphine (PH).
It is carried out by gas phase oxidizing a mixture of 3 ) and diborane (B 2 H 6 ) with a suitable inert diluent, typically nitrogen. Oxygen is the most commonly used oxidant, although other gases such as nitric oxide, nitrous oxide and carbon dioxide can be used. Normally, borophosphosilicate glass is about
It is deposited by chemical vapor deposition at a temperature of 410 ℃ ~ 450 ℃, about 4
25 ° C to about 430 ° C is the most typical temperature.

蒸着処理の温度を下げると、蒸着速度が５０％もしくは
それ以上改善されることを発見した。化学蒸着法による
蒸着は、蒸気の凝縮というよりもむしろ化学反応現象で
あるから、これは予想外なことである。すなわち、温度
を下げると、反応、従って、蒸着速度が遅くなるものと
考えられていた。特に、本発明によると、硼燐珪酸ガラ
スは、約３６０℃〜約３９０℃、望ましくは約３６５℃
〜約３７５℃の温度で化学蒸着法により蒸着される。最
も望ましい蒸着温度は、３７０℃である。ここで使用し
ている“化学蒸着法”という用語は、大気圧化学蒸着法
であって、蒸着を増強するためにプラズマを使う処理は
含んでいない。It has been discovered that lowering the temperature of the deposition process improves the deposition rate by 50% or more. This is unexpected because chemical vapor deposition is a chemical reaction phenomenon rather than vapor condensation. That is, it has been thought that when the temperature is lowered, the reaction and hence the vapor deposition rate slows down. In particular, according to the invention, the borophosphosilicate glass has a temperature of about 360 ° C to about 390 ° C, preferably about 365 ° C.
Deposited by chemical vapor deposition at a temperature of about 375 ° C. The most desirable vapor deposition temperature is 370 ° C. As used herein, the term "chemical vapor deposition" is atmospheric pressure chemical vapor deposition and does not include treatments that use plasma to enhance the vapor deposition.

本発明によって得られる第２の改良点は、従来の処理方
法により形成される硼燐珪酸ガラスの層中に存在する粒
子に関することである。組成は変わるかも知れないが、
主としてSiOxであるこれらの粒子は、均一気相核生成反
応から生ずるものであると考えられる。これらの粒子に
より硼燐珪酸ガラスの層が汚れ、またこれらの粒子が蒸
着槽の壁に付着する。このような粒子が蒸着槽の壁に付
着することは極めて重大な問題である。何故ならば、こ
のような付着が続いての蒸着の汚染源となるからであ
る。従って、蒸着装置を何回も洗浄しなければならず、
これは操作時間の損失となる。A second improvement obtained according to the invention relates to the particles present in the layer of borophosphosilicate glass formed by conventional processing methods. The composition may change,
These particles, predominantly SiO x , are believed to result from homogeneous gas phase nucleation reactions. These particles contaminate the layer of borophosphosilicate glass, and these particles adhere to the walls of the deposition bath. Adhesion of such particles to the wall of the deposition tank is a very serious problem. This is because such adhesion becomes a contamination source for the subsequent vapor deposition. Therefore, the vapor deposition apparatus must be washed many times,
This results in a loss of operating time.

酸素と水素化物との混合物中における酸素の量を増加さ
せると、硼燐珪酸ガラスの中において、また蒸着槽の壁
に汚染粒子の形成されるのが著しく低下することを発見
した。本発明によると、蒸着混合物中の酸素の量は、従
来の容積比の２０：１から、約３０：１と約６０：１の
間、望ましくは、約４０：１に増加される。これらの比
率は、酸素と全ての水素化物、すなわちシラン、ホスフ
インおよびジボラン全部との容積比である。一般に、酸
素の比率が大きくなると、蒸着速度に多大ではないが抑
制の影響が現われる。しかしながら、本発明によって実
現される蒸着速度の著しい増加により埋合わされる。It has been discovered that increasing the amount of oxygen in a mixture of oxygen and hydride significantly reduces the formation of contaminant particles in the borophosphosilicate glass and on the walls of the deposition chamber. According to the present invention, the amount of oxygen in the vapor deposition mixture is increased from a conventional volume ratio of 20: 1 to between about 30: 1 and about 60: 1, preferably about 40: 1. These ratios are the volume ratios of oxygen to all hydrides, ie silane, phosphine and diborane. Generally, as the proportion of oxygen increases, the effect of suppression appears, but not significantly, on the deposition rate. However, this is offset by the significant increase in deposition rate achieved by the present invention.

本発明に従って蒸着温度を下げることによっても硼燐珪
酸ガラスの層中の粒子による汚れを著しく低減させるこ
とができる。従って、ここで考えている処理の２つの改
良点により、粒子による汚れが減り、高純度で高品質の
硼燐珪酸ガラスの層が得られる。本発明に従って硼燐珪
酸ガラスの層を化学蒸着法で形成するのに特に適した条
件は、約３７０℃の蒸着温度、および酸素と全水素化物
の容積比が４０：１〜６０：１である。By lowering the vapor deposition temperature according to the present invention, it is possible to significantly reduce the contamination by particles in the borophosphosilicate glass layer. Thus, the two refinements of the process contemplated herein reduce particle contamination and provide a high purity, high quality layer of borophosphosilicate glass. Particularly suitable conditions for forming a layer of borophosphosilicate glass according to the present invention by chemical vapor deposition are a deposition temperature of about 370 ° C. and a volume ratio of oxygen to total hydride of 40: 1 to 60: 1. .

ここで考えている硼燐珪酸ガラスは、重量比で約３％〜
約６％の硼素、約２％〜約６％の燐を含んでいることが
適当であり、望ましくは、重量比で約４％〜約５％の硼
素、約３％〜約５％の燐を含んでいることが望ましい。
望ましいガラスとしては、重量比で約４％〜約４．５％
の硼素、約３．５％〜約４％の燐を含んでいるＡ型と、
重量比で約４．５％〜約５％の硼素、約４％〜約４．５
％の燐を含んでいるＢ型がある。本発明の処理方法によ
って得られる蒸着速度および膜品質の改良は、これらす
べての硼燐珪酸ガラスの組成物に適用できるものであ
る。The borophosphosilicate glass considered here is approximately 3% by weight.
Suitably it contains about 6% boron, about 2% to about 6% phosphorus, preferably about 4% to about 5% boron, about 3% to about 5% phosphorus. It is desirable to include.
The preferred glass is about 4% to about 4.5% by weight.
Boron, Form A containing about 3.5% to about 4% phosphorus,
About 4.5% to about 5% boron by weight, about 4% to about 4.5
There is B type which contains% phosphorus. The improvements in deposition rate and film quality obtained by the processing method of the present invention are applicable to all these borophosphosilicate glass compositions.

本発明による改良された処理方法の利点は、硼燐珪酸ガ
ラスの層についての著しく改善された蒸着速度である。
また、形成された層は極めて良好な均一性と純度を有す
る。さらに、気体源を効率的に使用することができ、ま
た装置の清浄と保守との間の増強された生産周期によ
り、安価に膜を形成することができる。また、本発明に
よる方法は特定の蒸着装置に必ずしも限定されないとい
う特徴がある。An advantage of the improved processing method according to the invention is the significantly improved deposition rate for layers of borophosphosilicate glass.
Also, the layers formed have very good uniformity and purity. Furthermore, the gas source can be used efficiently, and the enhanced production cycle between cleaning and maintenance of the device allows inexpensive film formation. Moreover, the method according to the present invention is not limited to a specific vapor deposition apparatus.

以下の例は本発明を示すものであるが、本発明はここに
詳細に開示したものに限定されるものではない。The following examples illustrate the invention, but the invention is not limited to the details disclosed herein.

例 １ 基板として３インチのシリコンウエハを使った例であ
る。アプライド・マテリアルズ株式会社（Applied Mate
rials Inc.）製のAMS−2100という反応装置を使って、
化学蒸着法により、１２枚の基板から成る各群につい
て、約8000Åの厚さに硼燐珪酸ガラスの層を蒸着させ
た。この場合の硼燐珪酸ガラスは、重量比で約４．５％
の硼素を含み、約４％の燐を含んでいるＢ型のものであ
った。Example 1 This is an example in which a 3-inch silicon wafer is used as a substrate. Applied Materials
AMS-2100 made by rials Inc.)
A layer of borophosphosilicate glass was deposited by chemical vapor deposition to a thickness of about 8000Å for each group of 12 substrates. In this case, borophosphosilicate glass is about 4.5% by weight.
Of type B with about 4% phosphorus.

４３０℃の蒸着温度を使って、酸素と全水素化物すなわ
ちシラン、ホスフィンおよびジボラン全部との容積比が
それぞれ２０：１，３０：１および４０：１なる蒸着混
合物から１２枚のウエハから成る各群に被着させた。平
均の粒子含有量を決定するために、浜松粒子計数装置を
使ってレーザー粒子走査により硼燐珪酸ガラスの層を検
査した。Each group consisting of 12 wafers from a deposition mixture having a volume ratio of oxygen to total hydrides, ie silane, phosphine and diborane of 20: 1, 30: 1 and 40: 1, respectively, using a deposition temperature of 430 ° C. It was applied to. The layer of borophosphosilicate glass was examined by laser particle scanning using a Hamamatsu particle counter to determine the average particle content.

酸素と全水素化物との容積比が２０：１の混合物を使っ
て蒸着した膜は、ウエハ当りの平均粒子数は４１９個で
あった。The film deposited using a 20: 1 volume ratio of oxygen to total hydride had an average particle number of 419 particles per wafer.

酸素と全水素化物との容積比が３０：１の混合物を使っ
て蒸着した膜は、ウエハ当りの平均粒子数が３４８個で
あり、また酸素と全水素化物との容積比が４０：１の混
合物を使って蒸着した膜は、ウエハ当りの平均粒子数が
１９５個であった。粒子の中の９０％のものは直径が
０．３μｍと２．０μｍ間にあり、直径が０．３μｍお
よび０．５μｍ間にあるものは８０％であった。The film deposited using a mixture of oxygen and total hydride in a volume ratio of 30: 1 has an average number of particles per wafer of 348 and a volume ratio of oxygen to total hydride of 40: 1. The film deposited with the mixture had an average number of particles per wafer of 195. 90% of the particles were between 0.3 μm and 2.0 μm in diameter, and 80% were between 0.3 μm and 0.5 μm in diameter.

この結果から、本発明により形成される硼燐珪酸ガラス
の層中の粒子による汚れが著しく改善されることが分
る。From this result, it can be seen that the contamination by particles in the layer of borophosphosilicate glass formed according to the present invention is remarkably improved.

例 ２ アールシーエー（ＲＣＡ）で製造したベルジャー回転型
反応装置を使って例１と同様に硼燐珪酸ガラスの層を３
インチのシリコンウエハに被着させた。この場合の硼燐
珪酸ガラスは、重量比で約４％の硼素と約３．５％の燐
を含んでいるＡ型のものであった。３枚のウエハから成
る各群は、酸素と全水素化物の容積比がそれぞれ２０：
１，３０：１，および６０：１なる混合物から被着され
た。Example 2 Three layers of borophosphosilicate glass were prepared in the same manner as in Example 1 using a bell jar rotary reactor manufactured by RCA.
It was deposited on an inch silicon wafer. The borophosphosilicate glass in this case was of type A containing about 4% boron and about 3.5% phosphorus by weight. Each group of 3 wafers has a volume ratio of oxygen to total hydride of 20:20.
It was applied from a mixture of 1,30: 1, and 60: 1.

ウエハの各群について、硼燐珪酸ガラスの層の蒸着速度
を通常の蒸着温度の４３０℃から２０℃あるいは３０℃
ずつ下げて３３０℃まで測定した。図は蒸着速度をプロ
ットしたものである。For each group of wafers, the deposition rate of the layer of borophosphosilicate glass was changed from the normal deposition temperature of 430 ° C to 20 ° C or 30 ° C.
The temperature was gradually lowered and measured up to 330 ° C. The figure is a plot of deposition rate.

図を参照すると、蒸着混合物中の酸素の容積が増加する
と硼燐珪酸ガラスの層の蒸着速度に幾分抑制効果の生ず
ることが分る。しかしながら、酸素の含有量が増えると
極めて純度の高い層の得られることが例１で示されてい
る。低い方の温度においては全ての比率で著しく増加し
た蒸着速度の得られることが図から分る。Referring to the figure, it can be seen that increasing the volume of oxygen in the deposition mixture has a somewhat inhibitory effect on the deposition rate of the layer of borophosphosilicate glass. However, Example 1 shows that an extremely high purity layer can be obtained when the oxygen content is increased. It can be seen from the figure that at all lower temperatures, significantly higher deposition rates are obtained.

例 ３ 例２で使った装置を使って、Ｂ型の硼燐珪酸ガラスの層
を何枚かのウエハから成る各群を被着した。すべての蒸
着において、酸素と全水素化物の容積比は４０：１であ
った。ウエハ当りの平均粒子数について、例２の場合と
同様に、４３０℃から始まって、１０℃間隔で下げてい
き３３０℃まで測定した。Example 3 Using the equipment used in Example 2, a layer of borophosphosilicate glass of type B was deposited on each group of several wafers. The volume ratio of oxygen to total hydride was 40: 1 in all depositions. The average number of particles per wafer was measured starting from 430 ° C. and decreasing at 10 ° C. intervals up to 330 ° C., as in Example 2.

３７０℃および３３０℃で被着したウエハは、４３０℃
で被着したものの平均粒子数よりもそれぞれ約７０％お
よび約７５％減少していた。これらの結果は、ここで考
察している蒸着温度によっても硼燐珪酸ガラスの層中の
粒子の量が実質的に減少し、従って、純度が改善される
ことを示すものである。Wafers deposited at 370 ° C and 330 ° C are 430 ° C
The number of particles deposited in No. 1 was reduced by about 70% and about 75%, respectively. These results show that the deposition temperatures discussed here also substantially reduce the amount of particles in the layer of borophosphosilicate glass, thus improving purity.

【図面の簡単な説明】[Brief description of drawings]

図は硼燐珪酸ガラスの蒸着速度を温度の関数で示したも
のである。The figure shows the deposition rate of borophosphosilicate glass as a function of temperature.

Claims (7)

【特許請求の範囲】[Claims] 【請求項１】酸素と、珪素、硼素および隣の各水素化物
との混合物を化学蒸着することにより適当な基板上に硼
燐珪酸ガラス層を形成する蒸着法であって、 蒸着が３６５°Ｃ〜３７５°Ｃの温度で行なわれ、前記
酸素と前記水素化物全部との容積比が４０：１〜６０：
１であることを特徴とする前記蒸着法。1. A vapor deposition method for forming a borophosphosilicate glass layer on a suitable substrate by chemical vapor deposition of a mixture of oxygen and silicon, boron and adjacent hydrides, the vapor deposition being 365 ° C. Is carried out at a temperature of ˜375 ° C., and the volume ratio of oxygen to all of the hydride is 40: 1˜60:
1. The vapor deposition method as described above. 【請求項２】蒸着が３７０°Ｃの温度で行なわれる特許
請求の範囲第１項記載の蒸着法。2. The vapor deposition method according to claim 1, wherein the vapor deposition is performed at a temperature of 370 ° C. 【請求項３】酸素と水素化物全部との容積比が４０：１
である特許請求の範囲第１項記載の蒸着法。3. The volume ratio of oxygen to all hydrides is 40: 1.
The vapor deposition method according to claim 1, wherein 【請求項４】蒸着が３７０°Ｃの温度で行なわれ、且つ
酸素と水素化物全部との容積比が４０：１である特許請
求の範囲第１項記載の蒸着法。4. The vapor deposition method according to claim 1, wherein the vapor deposition is carried out at a temperature of 370 ° C., and the volume ratio of oxygen to total hydride is 40: 1. 【請求項５】蒸着が３７０°Ｃの温度で行なわれ、且つ
酸素と水素化物全部との容積比が６０：１である特許請
求の範囲第１項記載の蒸着法。5. The vapor deposition method according to claim 1, wherein the vapor deposition is carried out at a temperature of 370 ° C., and the volume ratio of oxygen to total hydride is 60: 1. 【請求項６】混合物が不活性の希釈剤を含んでいる特許
請求の範囲第１項記載の蒸着法。6. A process according to claim 1, wherein the mixture contains an inert diluent. 【請求項７】前記希釈剤が窒素である特許請求の範囲第
６項記載の蒸着法。7. The vapor deposition method according to claim 6, wherein the diluent is nitrogen.
JP60171296A 1984-08-06 1985-08-05 Deposition method of borophosphosilicate glass Expired - Lifetime JPH066789B2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US636832 1984-08-06
US06/636,832 US4546016A (en) 1984-08-06 1984-08-06 Deposition of borophosphosilicate glass

Publications (2)

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JPS6144180A JPS6144180A (en) 1986-03-03
JPH066789B2 true JPH066789B2 (en) 1994-01-26

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3675415D1 (en) * 1985-03-11 1990-12-13 Applied Materials Inc MANUFACTURING PROCESS FOR BORPHOSPHORSILICATE GLASS.
ATE64237T1 (en) * 1985-05-22 1991-06-15 Siemens Ag PROCESS FOR MANUFACTURING BORON AND PHOSPHORUS-DOped SILICON COATINGS FOR SEMICONDUCTOR INTEGRATED CIRCUITS.
US4891247A (en) * 1986-09-15 1990-01-02 Watkins-Johnson Company Process for borosilicate glass films for multilevel metallization structures in semiconductor devices
US5268333A (en) * 1990-12-19 1993-12-07 Samsung Electronics Co., Ltd. Method of reflowing a semiconductor device
US5139209A (en) * 1991-04-29 1992-08-18 The Lincoln Electric Company Storage reel for welding wire
FR2698288B1 (en) * 1992-11-20 1994-12-23 Lair Liquide Gas supply process, in particular diborane and silane.
US5409743A (en) * 1993-05-14 1995-04-25 International Business Machines Corporation PECVD process for forming BPSG with low flow temperature
US5906861A (en) * 1993-07-20 1999-05-25 Raytheon Company Apparatus and method for depositing borophosphosilicate glass on a substrate
US5808353A (en) * 1996-06-20 1998-09-15 Harris Corporation Radiation hardened dielectric for EEPROM
US6087275A (en) * 1997-04-26 2000-07-11 Advanced Micro Devices, Inc. Reduction of n-channel parasitic transistor leakage by using low power/low pressure phosphosilicate glass
US6432564B1 (en) * 1999-08-12 2002-08-13 Mini Systems, Inc. Surface preparation of a substrate for thin film metallization
US6465373B1 (en) * 2000-08-31 2002-10-15 Micron Technology, Inc. Ultra thin TCS (SiCl4) cell nitride for DRAM capacitor with DCS (SiH2Cl2) interface seeding layer

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US3481781A (en) * 1967-03-17 1969-12-02 Rca Corp Silicate glass coating of semiconductor devices
US4349584A (en) * 1981-04-28 1982-09-14 Rca Corporation Process for tapering openings in ternary glass coatings
US4363830A (en) * 1981-06-22 1982-12-14 Rca Corporation Method of forming tapered contact holes for integrated circuit devices
US4433008A (en) * 1982-05-11 1984-02-21 Rca Corporation Doped-oxide diffusion of phosphorus using borophosphosilicate glass

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US4546016A (en) 1985-10-08
JPS6144180A (en) 1986-03-03

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